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Discontinuation of β-blocker therapy in stabilised patients after acute myocardial infarction (SMART-DECISION): rationale and design of the randomised controlled trial

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Author(s)
Ki Hong ChoiJuwon KimDanbee KangJoon-Hyung DohJuhan KimYong Hwan ParkSung Gyun AhnWeon KimJong Pil ParkSang Min KimByung-Ryul ChoChang-Wook NamJang Hyun ChoSeung-Jae JooJon SuhJin-Ok JeongWoo JangChang-Hwan YoonJin-Yong HwangSeong-Hoon LimSang-Rok LeeEun-Seok ShinByung Jin KimCheol Woong YuSung-Ho HerHyun Kuk KimKyu Tae ParkJihoon KimTaek Kyu ParkJoo-Myung LeeJuhee ChoJeong Hoon YangYoung Bin SongSeung Hyuk ChoiHyeon-Cheol GwonEliseo GuallarJoo-Yong Hahn
Keimyung Author(s)
Nam, Chang Wook
Department
Dept. of Internal Medicine (내과학)
Journal Title
BMJ Open
Issued Date
2024
Volume
14
Issue
8
Abstract
Introduction:
There is a lack of evidence to support the effectiveness of prolonged β-blocker therapy after stabilisation of patients with acute myocardial infarction (AMI) without heart failure (HF) or left ventricular systolic dysfunction.

Methods and analysis:
The SMart Angioplasty Research Team: DEcision on Medical Therapy in Patients with Coronary Artery DIsease or Structural Heart Disease Undergoing InterventiON (SMART-DECISION) trial is a multicentre, prospective, open-label, randomised, non-inferiority trial designed to determine whether discontinuing β-blocker therapy after ≥1 year of maintenance in stabilised patients after AMI is non-inferior to continuing it. Patients eligible for participation are those without HF or left ventricular systolic dysfunction (ejection fraction >40%) who have been continuing β-blocker therapy for ≥1 year after AMI. A total of 2540 patients will be randomised 1:1 to continuation of β-blocker therapy or not. Randomisation will be stratified according to the type of AMI (ie, ST-segment-elevation MI or non-ST-segment-elevation MI), type of β-blocker (carvedilol, bisoprolol, nebivolol or other) and participating centre. The primary study endpoint is a composite of all-cause death, MI and hospitalisation for HF over a median follow-up period of 3.5 years (minimum, 2.5 years; maximum, 4.5 years). Adverse effects related to β-blocker therapy, the occurrence of atrial fibrillation, medical costs and Patient-reported Outcomes Measurement Information system-29 questionnaire responses will also be collected as secondary endpoints.

Ethics and dissemination:
Ethics approval for this study was granted by the Institutional Review Board of Samsung Medical Center (no. 2020-10-176). Informed consent is obtained from every participant before randomisation. The results of this study will be submitted for publication in international peer-reviewed journals and the key findings will be presented at international scientific conferences.
Keimyung Author(s)(Kor)
남창욱
Publisher
School of Medicine (의과대학)
Type
Article
ISSN
2044-6055
Source
https://bmjopen.bmj.com/content/14/8/e086971.long
DOI
10.1136/bmjopen-2024-086971
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/45850
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
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